Author:
Bianco Suzy D. C.,Kaiser Ursula B.
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference75 articles.
1. Cadman, S. M., Kim, S. H., Hu, Y., González-Martínez, D. & Bouloux, P. M. Molecular pathogenesis of Kallmann's syndrome. Horm. Res. 67, 231–242 (2007).
2. Schwanzel-Fukuda, M. Origin and migration of luteinizing hormone-releasing hormone neurons in mammals. Microsc. Res. Tech. 44, 2–10 (1999).
3. Cariboni, A. & Maggi, R. Kallmann's syndrome, a neuronal migration defect. Cell. Mol. Life Sci. 63, 2512–2526 (2006).
4. Pitteloud, N. et al. Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism. Proc. Natl Acad. Sci. USA 103, 6281–6286 (2006).
5. Pitteloud, N. et al. Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes. Mol. Cell Endocrinol. 254–255, 60–69 (2006).
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